Oxysurf 0.25 % Solution ; Spray is a Health Canada–registered disinfectant drug (DIN 02544717) held by Osorno Enterprises Inc., containing Sodium Chlorite. Health Canada lists its status as Approved (status date 19 Jan 2024). Nexara Health has matched 11 registrations of Sodium Chlorite across 1 other regulated market.
Health Canada registration
| DIN | 02544717 |
|---|---|
| Brand name | Oxysurf |
| Active ingredient | Sodium Chlorite |
| Strength | 0.25 % |
| Dosage form | Solution ; Spray |
| Route | DISINFECTANT (Barn) ; DISINFECTANT (Domestic) ; DISINFECTANT (Hospital/HC Facilities) ; DISINFECTANT (Institutional/Industrial) |
| Company | Osorno Enterprises Inc. |
| Status | Approved — 19 Jan 2024 |
| Class | Disinfectant |
| ATC | V07AV TECHNICAL DISINFECTANTS |
| AHFS | |
| Regulator record | Health Canada DPD entry · Product monograph |
Sodium Chlorite registered in other markets
11 registrations of the same molecule in 1 national registry outside Canada (first 8 shown, exact strength and form first). Each row is taken from the regulator's own published list; status is shown as the registry reports it.
| Country | Product | Marketing authorisation holder | Strength | Form | Status | Registry |
|---|---|---|---|---|---|---|
| United States | D.PRO Pack Solid | Pure O2 | Powder | listed | FDA NDC | |
| United States | Defender Signature | Pure O2 | Powder | listed | FDA NDC | |
| United States | Defenderstick | Pure O2 | Liquid | listed | FDA NDC | |
| United States | Doctor GuardStick | Pure O2 | Liquid | listed | FDA NDC | |
| United States | EasyStick | Pure O2 | Liquid | listed | FDA NDC | |
| United States | iSTICK | Pure O2 | Liquid | listed | FDA NDC | |
| United States | NARYN CARE Stick | Pure O2 | Liquid | listed | FDA NDC | |
| United States | PURE O2 Pack-Solid | Pure O2 | Powder | listed | FDA NDC |
See every manufacturer of Sodium Chlorite worldwide →
Related molecules (ATC V07AV)
- Alcohol Anhydrous
- Alcohol Denatured
- Alkyl Dimethyl Benzyl Ammonium Saccharinate
- Alkyl Dimethyl Ethylbenzyl Ammonium Chloride
- Benzalkonium Chloride
Sourcing through Nexara Health
Nexara Health is a Health Canada–licensed wholesaler (DEL #3-002896) in Winnipeg. This DIN is not currently marketed in Canada. The registrations above show which regulated markets hold an equivalent presentation that can be sourced for clinical comparator use or on a named-patient basis under Health Canada's Special Access Programme. Request a quote or read how named-patient and foreign-pack supply works in Canada.
Frequently asked questions
Is Oxysurf (DIN 02544717) marketed in Canada?
No. Health Canada lists DIN 02544717 as Approved as of 19 Jan 2024.
Who holds the Canadian licence for this product?
Osorno Enterprises Inc. is the company of record in the Health Canada Drug Product Database.
Is Sodium Chlorite registered outside Canada?
Yes — Nexara Health has matched 11 registrations in 1 other market (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 02544717, status date 2024-01-19; national medicine registries: FDA NDC. Nexara Health re-checks these sources weekly and shows the last verification date at the top of the page.
Source: Health Canada Drug Product Database (DPD), DIN 02544717, status date 2024-01-19; national medicine registries: FDA NDC.
Health Canada Drug Product Database (DPD), DIN 02544717, status date 2024-01-19; national medicine registries: FDA NDC. Last reviewed 2026-09-17. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.